chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104775534247755343CT35GENIChomozygous52459527
104775629747756298GA47GENIChomozygous52459528
104775647147756472TC31GENIChomozygous51446413
104775772347757724AG35GENICpossibly homozygous51446414
104775980247759808TTTTTT------7GENICheterozygous51638445
104775980547759808TTT---7GENICheterozygous52374042
104776038147760383TC--8GENICheterozygous52459529
104776133747761338TTGG8GENIChomozygous52459530
104776161547761616TG34GENIChomozygous51446418
104776234547762346GGTTT13GENICheterozygous51638447
104776324147763242TC36GENIChomozygous52459531
104776590047765901A-32GENIChomozygous52459532
104776769047767691T-26GENIChomozygous52459533
104776850347768504AAC36GENIChomozygous51446421
104776861747768618AG39GENIChomozygous51446422
104777025447770255TC33GENIChomozygous51446423
104777032947770330GA31GENICpossibly homozygous52459534
104777441947774423ACAC----1GENIChomozygous52374044
104777532147775322GA39GENIChomozygous52459535